Job Description

• Growing Fortune 500 pharmaceutical organization

• Cross functional and regional collaboration

• Exciting career progression path

Responsibilities:

• Perform quality oversight of RDC operations (bottle labeling, secondary packaging, redressing, warehousing and distribution) of products in Asia RDC and ensure its compliance to applicable regulatory requirements to support continuous operations of RDC and continuous provision of quality compliant products.

• Manage/perform quality operations/activities for RDC operations and ensure its compliance to applicable regulatory requirements to support continuous operations of RDC and continuous provision of quality compliant products.

• Develop, implement and maintain a fit for purpose Quality Management System (QMS) as per applicable regulatory requirements and to support continuous operations of RDC and continuous provision of quality compliant products.

• Management of all relevant regulatory and/or certification inspections/audits for RDC to ensure successful maintenance/renewal of licenses/certifications.

• Management of all external/internal audit program for RDC as per applicable regulatory requirements.

• Perform/support quality activities for timely resolution of product/quality issues related to RDC.

• Perform/support quality activities timely and as per all applicable regulatory requirements for all relevant post marketing activities related to product packaged in RDC.

• Provide quality input/support timely for relevant business projects, initiatives and requests, new product introduction, product launches, product variation if needed. Provide support to other Asia QA members or Asia countries quality operations if needed.

• Manage QA operation budget for RDC.

• Conduct internal and external audits as required

Requirements:

• At least 3-5 years of quality assurance working experience in pharmaceutical industry.

• RDC experience is advantageous

• Degree in pharmacy, or relevant discipline.

• Working knowledge of GMP and GDP in the pharmaceutical industry

• Motivated and driven personality

How to Apply:

• Interested applicants may apply by sending in your updated r\xc3\xa9sum\xc3\xa9 (in MS Word format) to my email or apply directly:

• Consultant: Tan Wei Xiang

• EA personnel reg. no.- R1658660

• EA License No. 17C8502

Additional Information

Career Level

Senior Executive

Qualification

Diploma, Advanced/Higher/Graduate Diploma, Bachelor\'s Degree, Post Graduate Diploma, Professional Degree, Master\'s Degree

Years of Experience

4 years

Job Type

Full-Time

Job Specializations

,

Company Overview

Meet Integrity. We\'re a leading recruitment firm specializing in the areas of Life Sciences and Engineering with over 100 years of combined experience in the industry. We\'ve helped recruit the most prized talent in a wide variety of Life Science and Construction sectors.

With 40% of our waking time dedicated to work, we know the vital importance of how smallest actions can create the biggest impact in people\'s lives. This is exactly why our friendly team of skilled experts always prioritizes actions based on core values over personal gain.

The secret to our business is personal relationships. Because People Matter.

We\'ve been very fortunate to assist with the recruitment of some of the most talented and dynamic talent for many of the largest and smallest employers. These are businesses who were in need of elite recruits who possessed specific talents, unique skills and other technical disciplines. Reach out to us to to discover even more about how we can help you with all of your recruiting needs or your own career.

Additional Company Information

Registration No.

201634573Z

EA No.

17C8502

Company Size

1 - 50 Employees

Industry

Human Resources Management / Consulting

Benefits & Others

Miscellaneous allowance, Long hours, Formal (e.g. Shirts + Ties)

Integrity Partners